Magnetism and magnetoelectricity in the polar oxide α-Cu2V2O7

Single crystals of the orthorhombic polar oxide α-Cu2V2O7 with space group Fdd2 are synthesized and their physical properties are measured. Neutron powder diffraction is also performed on a polycrystal sample to extract the magnetic structure. The ground state is shown to be weakly ferromagnetic, th...

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Published inEurophysics letters Vol. 113; no. 2; pp. 27007 - 27012
Main Authors Lee, Y.-W., Jang, T.-H., Dissanayake, S. E., Lee, Seunghun, Jeong, Yoon H.
Format Journal Article
LanguageEnglish
Published Les Ulis EDP Sciences, IOP Publishing and Società Italiana di Fisica 01.01.2016
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Abstract Single crystals of the orthorhombic polar oxide α-Cu2V2O7 with space group Fdd2 are synthesized and their physical properties are measured. Neutron powder diffraction is also performed on a polycrystal sample to extract the magnetic structure. The ground state is shown to be weakly ferromagnetic, that is, collinearly antiferromagnetic in the a-direction with a small remanent magnetization in the c-direction. When an external magnetic field is applied in the c-direction, further spin canting, accompanied by the induced electric polarization, occurs. It is demonstrated that the magnetoelectric effect in α-Cu2V2O7 is adequately described if spin-dependent hybridization due to spin-orbit coupling as well as magnetic domain effects are simultaneously taken into account. We discuss the implication of the present result in the search for materials with multiferroicity and/or magnetoelectricity.
AbstractList Single crystals of the orthorhombic polar oxide α-Cu2V2O7 with space group Fdd2 are synthesized and their physical properties are measured. Neutron powder diffraction is also performed on a polycrystal sample to extract the magnetic structure. The ground state is shown to be weakly ferromagnetic, that is, collinearly antiferromagnetic in the a-direction with a small remanent magnetization in the c-direction. When an external magnetic field is applied in the c-direction, further spin canting, accompanied by the induced electric polarization, occurs. It is demonstrated that the magnetoelectric effect in α-Cu2V2O7 is adequately described if spin-dependent $p\text{-}d$ hybridization due to spin-orbit coupling as well as magnetic domain effects are simultaneously taken into account. We discuss the implication of the present result in the search for materials with multiferroicity and/or magnetoelectricity.
Single crystals of the orthorhombic polar oxide α-Cu2V2O7 with space group Fdd2 are synthesized and their physical properties are measured. Neutron powder diffraction is also performed on a polycrystal sample to extract the magnetic structure. The ground state is shown to be weakly ferromagnetic, that is, collinearly antiferromagnetic in the a-direction with a small remanent magnetization in the c-direction. When an external magnetic field is applied in the c-direction, further spin canting, accompanied by the induced electric polarization, occurs. It is demonstrated that the magnetoelectric effect in α-Cu2V2O7 is adequately described if spin-dependent hybridization due to spin-orbit coupling as well as magnetic domain effects are simultaneously taken into account. We discuss the implication of the present result in the search for materials with multiferroicity and/or magnetoelectricity.
Author Jeong, Yoon H.
Lee, Y.-W.
Dissanayake, S. E.
Lee, Seunghun
Jang, T.-H.
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  organization: Pohang University of Science and Technology Department of Physics, - Pohang, 790-784, Korea
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Snippet Single crystals of the orthorhombic polar oxide α-Cu2V2O7 with space group Fdd2 are synthesized and their physical properties are measured. Neutron powder...
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SubjectTerms 75.10.-b
75.25.-j
75.85.+t
Antiferromagnetism
Electric polarization
Ferromagnetism
Magnetic domains
Magnetic properties
Magnetic structure
Neutron diffraction
Physical properties
Polarization (spin alignment)
Polycrystals
Single crystals
Spin-orbit interactions
Title Magnetism and magnetoelectricity in the polar oxide α-Cu2V2O7
URI https://iopscience.iop.org/article/10.1209/0295-5075/113/27007
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